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Bioseal Inc.

FDA UDI

Class II (US FDA UDI)

by Bioseal

Identity

Trade Name
Bioseal Inc. FDA UDI
Generic Name
Polypectomy endoscopic ligator, single-use FDA UDI
Device Name
Hemorrhoid Bands FDA UDI
Model / Reference
18006/20 FDA UDI
Description
Hemorrhoid Bands FDA UDI

Identifiers

Primary DI / UDI-DI
00630094180069 FDA UDI
FDA Product Code
FHN FDA UDI
GMDN Term
Polypectomy endoscopic ligator, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Polypectomy endoscopic ligator, single-use

Bioseal Inc. by Bioseal — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Polypectomy endoscopic ligator, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bioseal

Sources (1)

  • FDA UDI 8db77a7c-de45-4b8f-a18b-9487b7e91572 33 fields · synced May 30, 2026